Literature DB >> 9396798

CDF-1-mediated repression of cell cycle genes targets a specific subset of transactivators.

J Zwicker1, F C Lucibello, V Jérôme, S Brüsselbach, R Müller.   

Abstract

The cdc25C , cyclin A and cdc2 genes are regulated during the cell cycle through two contiguous repressor binding sites, the CDE and CHR, located in the region of transcription initiation and interacting with a factor termed CDF-1. The target of this repression seems to be transcriptional activation of these promoters by transcription factors bound upstream. The majority of these factors falls into the class of glutamine-rich activators, suggesting that CDF-1-mediated repression might be activation domain specific. In the present study we have used chimeric promoter constructs to demonstrate that the cdc25C UAS, but not the core promoter, is crucial for repression. In addition, we show that only specific transcription factors and activation domains are responsive to CDE-CHR-mediated cell cycle regulation. These observations clearly indicate that CDF-1 interferes with activation of transcription by a specific subset of transactivators. The repressible activation domains belong to the same class of glutamine-rich activators, pointing to specific interactions of CDF-1 with components of the transcription machinery. In agreement with this conclusion we find that a simple inversion of the CDE-CHR module completely abrogates cell cycle-regulated repression.

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Year:  1997        PMID: 9396798      PMCID: PMC147152          DOI: 10.1093/nar/25.24.4926

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  52 in total

1.  Repression of p53-mediated transcription by MDM2: a dual mechanism.

Authors:  C J Thut; J A Goodrich; R Tjian
Journal:  Genes Dev       Date:  1997-08-01       Impact factor: 11.361

2.  Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle.

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3.  Direct transcriptional repression by pRB and its reversal by specific cyclins.

Authors:  R Bremner; B L Cohen; M Sopta; P A Hamel; C J Ingles; B L Gallie; R A Phillips
Journal:  Mol Cell Biol       Date:  1995-06       Impact factor: 4.272

Review 4.  Transcriptional regulation during the mammalian cell cycle.

Authors:  R Müller
Journal:  Trends Genet       Date:  1995-05       Impact factor: 11.639

Review 5.  The price of repression.

Authors:  A D Johnson
Journal:  Cell       Date:  1995-06-02       Impact factor: 41.582

6.  Basal promoter elements as a selective determinant of transcriptional activator function.

Authors:  G Das; C S Hinkley; W Herr
Journal:  Nature       Date:  1995-04-13       Impact factor: 49.962

7.  Recombinant rat CBF-C, the third subunit of CBF/NFY, allows formation of a protein-DNA complex with CBF-A and CBF-B and with yeast HAP2 and HAP3.

Authors:  S Sinha; S N Maity; J Lu; B de Crombrugghe
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-28       Impact factor: 11.205

8.  Mechanism of active transcriptional repression by the retinoblastoma protein.

Authors:  S J Weintraub; K N Chow; R X Luo; S H Zhang; S He; D C Dean
Journal:  Nature       Date:  1995-06-29       Impact factor: 49.962

9.  Control of transcription by Krüppel through interactions with TFIIB and TFIIE beta.

Authors:  F Sauer; J D Fondell; Y Ohkuma; R G Roeder; H Jäckle
Journal:  Nature       Date:  1995-05-11       Impact factor: 49.962

10.  Periodic cdc25C transcription is mediated by a novel cell cycle-regulated repressor element (CDE).

Authors:  F C Lucibello; M Truss; J Zwicker; F Ehlert; M Beato; R Müller
Journal:  EMBO J       Date:  1995-01-03       Impact factor: 11.598

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  3 in total

1.  Timing of cyclin E gene expression depends on the regulated association of a bipartite repressor element with a novel E2F complex.

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Journal:  EMBO J       Date:  1999-04-01       Impact factor: 11.598

2.  E2 Ubiquitin-conjugating Enzyme, UBE2C Gene, Is Reciprocally Regulated by Wild-type and Gain-of-Function Mutant p53.

Authors:  Swati Bajaj; Sk Kayum Alam; Kumar Singha Roy; Arindam Datta; Somsubhra Nath; Susanta Roychoudhury
Journal:  J Biol Chem       Date:  2016-04-28       Impact factor: 5.157

3.  Cyclin-dependent kinase-associated proteins Cks1 and Cks2 are essential during early embryogenesis and for cell cycle progression in somatic cells.

Authors:  Hanna-Stina Martinsson-Ahlzén; Vasco Liberal; Björn Grünenfelder; Susana R Chaves; Charles H Spruck; Steven I Reed
Journal:  Mol Cell Biol       Date:  2008-07-14       Impact factor: 4.272

  3 in total

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